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Ceftazidime- and Imipenem-Induced Endotoxin Release During Treatment of Gram-Negative Infections

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European Journal of Clinical Microbiology & Infectious Diseases Aims and scope Submit manuscript

Abstract.

To determine whether ceftazidime and imipenem, which target two different penicillin-binding proteins, result in different amounts of endotoxin and cytokine release in patients with gram-negative infection, plasma endotoxin, interleukin-6, and tumor necrosis factor alpha were measured during the first 24 h of antibiotic therapy in 27 patients with gram-negative infection who had been randomized to receive either ceftazidime 2 g t.i.d. (n=12) or imipenem/cilastatin 1 g t.i.d. (n=15). The source of infection was the digestive tract (n=13), the urinary tract (n=5), the respiratory tract (n=2), soft tissue (n=2), i.v. line (n=2), or other (n=3). After the first antibiotic injection, a significant increase in the median concentration of plasma interleukin-6 and plasma tumor necrosis factor alpha was noted, without significant differences related to the antibiotic administered. Antibiotic-induced endotoxemia was detectable in nine patients (including 7 with bacteremia). In conclusion, ceftazidime and imipenem had similar effects on endotoxin and cytokine release during the treatment of gram-negative infections.

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Byl, B., Clevenbergh, P., Kentos, A. et al. Ceftazidime- and Imipenem-Induced Endotoxin Release During Treatment of Gram-Negative Infections. Eur J Clin Microbiol Infect Dis 20, 804–807 (2001). https://doi.org/10.1007/s100960100609

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  • DOI: https://doi.org/10.1007/s100960100609

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